Experimental detection of urinary protein by heated acetic acid method
Heating can denature the protein and solidify it, and adding acid can make the protein close to the isoelectric point, which can lead to the precipitation of th
3,200+ step-by-step lab protocols and SOPs for cell culture, staining, PCR, protein work and microbiology, with reagents, conditions and evaluation criteria.
Heating can denature the protein and solidify it, and adding acid can make the protein close to the isoelectric point, which can lead to the precipitation of th
In the reagent tape there is no glucose oxidase (GOD) peroxidase (POD) pigment original and weak acidic buffer composed of the reaction reagent and as the base
Sulfosalicylic acid is an alkaloidal reagent, the cation of the protein amino group on the acidic sulfonate ion combines to form an insoluble protein salt preci
Heating can denature the protein and solidify it, and adding acid can make the protein close to the isoelectric point, which can lead to the precipitation of th
Lab Notes: 1. The fresh pH value of urine should be below 6. 2, the examined urine SG in 1.026 or less, such as <1.016 for hypotonic urine easy to destroy
Is based on the working principle of flow cytometry designed for urine sediment analysis, this type of instrument is less expensive, higher analytical efficienc
There are latex agglutination test and blood inhibition test, radioimmunoassay (RIA), enzyme-linked immunosorbent assay (ELISA), monoclonal antibody colloidal g
1, clean slides with isotonic saline for 1-2 d, selecting abnormal parts of the feces, or selecting different parts of the feces to be directly smeared. 2. It
In recent years, enzyme immunoassay technology has developed rapidly. The methods of HCG detection are endless. At present, the detection methods applying enzym